Cinnafresh by Bob Barker Company Inc. Cinnafresh

Cinnafresh by

Drug Labeling and Warnings

Cinnafresh by is a Otc medication manufactured, distributed, or labeled by Bob Barker Company Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

CINNAFRESH- sodium fluoride gel, dentifrice 
Bob Barker Company Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Cinnafresh

DRUG FACTS

ACTIVE INGREDIENT

Sodium fluoride- 0.22% (0.1% w/v fluoride ion)

PURPOSE

Anticavity

USE

Helps protect against cavities.

WARNINGS

Keep out of reach of children under 6 years of age. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center immediately.

DIRECTIONS

Adults & children 6 years of age & older:Brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or physician.
Children 2 to 6 years: Use only a pea sized amount and supervise child's brushing and rinsing (to minimize swallowing).
Children under 2 years:Ask a dentist or physician.

INACTIVE INGREDIENTS

Purified Water, Sorbitol, Carbopol, Sodium Lauryl Sulphate, Flavor, Poly Ethylene Glycol 1500, Sodium Saccharin, Precipitated Silica, Sodium Carboxy Methyl Cellulose, Methyl Paraben, Propyl Paraben, FD & C Red # 40.

PRINCIPAL DISPLAY PANEL - 24 GRAM Tube Label

CinnaFresh
anticavity gel toothpaste

NET WT. 0.85 OZ
(24 GRAMS)

Principal Display Panel - 24 GRAM Tube Label
CINNAFRESH 
sodium fluoride gel, dentifrice
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 53247-110
Route of AdministrationDENTAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION2.2 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SORBITOL (UNII: 506T60A25R)  
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
POLYETHYLENE GLYCOL 1500 (UNII: 1212Z7S33A)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 53247-110-0124 g in 1 TUBE; Type 0: Not a Combination Product01/01/200812/01/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35501/01/200812/01/2019
Labeler - Bob Barker Company Inc. (058525536)

Revised: 2/2020
Document Id: 9eedf5b9-2122-8299-e053-2995a90ab2f9
Set id: c0191a1c-c849-4dc8-b823-3c9f287f243a
Version: 3
Effective Time: 20200219
 
Bob Barker Company Inc.